Yayın:
New 1,3,4-thiadiazole compounds including pyrazine moiety: Synthesis, structural properties and antimicrobial features

dc.contributor.authorGür, Mahmut
dc.contributor.authorŞener, Nesrin
dc.contributor.authorMuğlu, Halit
dc.contributor.authorÇavuş, M. Serdar
dc.contributor.authorÖzkan, Osman Emre
dc.contributor.authorKandemirli, Fatma
dc.contributor.authorŞener, İzzet
dc.date.accessioned2026-01-03T10:05:58Z
dc.date.issued2017-07-01
dc.description.abstractAbstract In the study, some new 1,3,4-thiadiazole compounds were synthesized and we have reported identification of the structures by using UV-Vis, FT-IR, 1H NMR, 13C NMR and Mass spectroscopic methods. Antimicrobial activities of the compounds against three microorganisms, namely, Candida albicans ATCC 26555, Staphylococcus aureus ATCC 9144, and Escherichia coli ATCC 25922 were investigated by using disk diffusion method. These thiadiazoles exhibited an antimicrobial activity against Staphylococcus aureus and Candida albicans. The experimental data was supported by the quantum chemical calculations. Density functional theory (DFT) calculations were carried out to obtain the ground state optimized geometries of the molecules using the B3LYP, M06 and PBE1PBE methods with 3–21 g, 4–31 g, 6–311++g(2d,2p), cc-pvtz and cc-pvqz basis sets in the different combinations. Frontier molecular orbitals (FMOs) energies, band gap energies and some chemical reactivity parameters were calculated by using the aforementioned methods and basis sets, and the results were also compared with the experimental UV-Vis data.
dc.description.urihttps://doi.org/10.1016/j.molstruc.2017.03.019
dc.description.urihttps://dx.doi.org/10.1016/j.molstruc.2017.03.019
dc.identifier.doi10.1016/j.molstruc.2017.03.019
dc.identifier.endpage118
dc.identifier.issn0022-2860
dc.identifier.openairedoi_dedup___::d515d92e7053c8ec2933cbeb1d384f66
dc.identifier.orcid0000-0001-9942-6324
dc.identifier.orcid0000-0001-5370-6048
dc.identifier.orcid0000-0002-3721-0883
dc.identifier.orcid0000-0003-4011-8815
dc.identifier.orcid0000-0003-0540-7523
dc.identifier.scopus2-s2.0-85015079391
dc.identifier.startpage111
dc.identifier.urihttps://hdl.handle.net/20.500.12597/36482
dc.identifier.volume1139
dc.identifier.wos000400718500012
dc.language.isoeng
dc.publisherElsevier BV
dc.relation.ispartofJournal of Molecular Structure
dc.rightsCLOSED
dc.subject.sdg3. Good health
dc.titleNew 1,3,4-thiadiazole compounds including pyrazine moiety: Synthesis, structural properties and antimicrobial features
dc.typeArticle
dspace.entity.typePublication
local.api.response{"authors":[{"fullName":"Mahmut Gür","name":"Mahmut","surname":"Gür","rank":1,"pid":{"id":{"scheme":"orcid","value":"0000-0001-9942-6324"},"provenance":null}},{"fullName":"Nesrin Şener","name":"Nesrin","surname":"Şener","rank":2,"pid":{"id":{"scheme":"orcid_pending","value":"0000-0001-5370-6048"},"provenance":null}},{"fullName":"Halit Muğlu","name":"Halit","surname":"Muğlu","rank":3,"pid":null},{"fullName":"M. Serdar Çavuş","name":"M. Serdar","surname":"Çavuş","rank":4,"pid":{"id":{"scheme":"orcid","value":"0000-0002-3721-0883"},"provenance":null}},{"fullName":"Osman Emre Özkan","name":"Osman Emre","surname":"Özkan","rank":5,"pid":{"id":{"scheme":"orcid","value":"0000-0003-4011-8815"},"provenance":null}},{"fullName":"Fatma Kandemirli","name":"Fatma","surname":"Kandemirli","rank":6,"pid":null},{"fullName":"İzzet Şener","name":"İzzet","surname":"Şener","rank":7,"pid":{"id":{"scheme":"orcid","value":"0000-0003-0540-7523"},"provenance":null}}],"openAccessColor":null,"publiclyFunded":false,"type":"publication","language":{"code":"eng","label":"English"},"countries":null,"subjects":[{"subject":{"scheme":"FOS","value":"01 natural sciences"},"provenance":null},{"subject":{"scheme":"SDG","value":"3. Good health"},"provenance":null},{"subject":{"scheme":"FOS","value":"0104 chemical sciences"},"provenance":null}],"mainTitle":"New 1,3,4-thiadiazole compounds including pyrazine moiety: Synthesis, structural properties and antimicrobial features","subTitle":null,"descriptions":["Abstract In the study, some new 1,3,4-thiadiazole compounds were synthesized and we have reported identification of the structures by using UV-Vis, FT-IR, 1H NMR, 13C NMR and Mass spectroscopic methods. Antimicrobial activities of the compounds against three microorganisms, namely, Candida albicans ATCC 26555, Staphylococcus aureus ATCC 9144, and Escherichia coli ATCC 25922 were investigated by using disk diffusion method. These thiadiazoles exhibited an antimicrobial activity against Staphylococcus aureus and Candida albicans. The experimental data was supported by the quantum chemical calculations. Density functional theory (DFT) calculations were carried out to obtain the ground state optimized geometries of the molecules using the B3LYP, M06 and PBE1PBE methods with 3–21 g, 4–31 g, 6–311++g(2d,2p), cc-pvtz and cc-pvqz basis sets in the different combinations. Frontier molecular orbitals (FMOs) energies, band gap energies and some chemical reactivity parameters were calculated by using the aforementioned methods and basis sets, and the results were also compared with the experimental UV-Vis data."],"publicationDate":"2017-07-01","publisher":"Elsevier BV","embargoEndDate":null,"sources":["Crossref"],"formats":null,"contributors":null,"coverages":null,"bestAccessRight":{"code":"c_14cb","label":"CLOSED","scheme":"http://vocabularies.coar-repositories.org/documentation/access_rights/"},"container":{"name":"Journal of Molecular Structure","issnPrinted":"0022-2860","issnOnline":null,"issnLinking":null,"ep":"118","iss":null,"sp":"111","vol":"1139","edition":null,"conferencePlace":null,"conferenceDate":null},"documentationUrls":null,"codeRepositoryUrl":null,"programmingLanguage":null,"contactPeople":null,"contactGroups":null,"tools":null,"size":null,"version":null,"geoLocations":null,"id":"doi_dedup___::d515d92e7053c8ec2933cbeb1d384f66","originalIds":["S0022286017302806","10.1016/j.molstruc.2017.03.019","50|doiboost____|d515d92e7053c8ec2933cbeb1d384f66","2605152343"],"pids":[{"scheme":"doi","value":"10.1016/j.molstruc.2017.03.019"}],"dateOfCollection":null,"lastUpdateTimeStamp":null,"indicators":{"citationImpact":{"citationCount":23,"influence":3.5107675e-9,"popularity":1.1143692e-8,"impulse":11,"citationClass":"C4","influenceClass":"C4","impulseClass":"C4","popularityClass":"C4"}},"instances":[{"pids":[{"scheme":"doi","value":"10.1016/j.molstruc.2017.03.019"}],"license":"Elsevier TDM","type":"Article","urls":["https://doi.org/10.1016/j.molstruc.2017.03.019"],"publicationDate":"2017-07-01","refereed":"peerReviewed"},{"alternateIdentifiers":[{"scheme":"mag_id","value":"2605152343"},{"scheme":"doi","value":"10.1016/j.molstruc.2017.03.019"}],"type":"Article","urls":["https://dx.doi.org/10.1016/j.molstruc.2017.03.019"],"refereed":"nonPeerReviewed"}],"isGreen":false,"isInDiamondJournal":false}
local.import.sourceOpenAire
local.indexed.atWOS
local.indexed.atScopus

Dosyalar

Koleksiyonlar